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Displaying 11 results.
    • Journal article
    A novel splicing mutation in SLC12A3 associated with Gitelman syndrome and idiopathic intracranial hypertension.
    Godefroid, Nathalie Riveira-Munoz, Eva[UCL] Saint-Martin, Christine Nassogne, Marie-Cécile[UCL] Dahan, Karin[UCL] Devuyst, Olivier[UCL] (2006) American journal of kidney diseases : the official journal of the National Kidney Foundation — Vol. 48, no. 5, p. e73-9 (2006)
    • Journal article
    Defects in KCNJ16 Cause a Novel Tubulopathy with Hypokalemia, Salt Wasting, Disturbed Acid-Base Homeostasis, and Sensorineural Deafness
    Schlingmann, Karl P. Renigunta, Aparna Hoorn, Ewout J. Forst, Anna-Lena Renigunta, Vijay Atanasov, Velko Mahendran, Sinthura Barakat, Tahsin Stefan Gillion, Valentine[UCL] Godefroid, Nathalie[UCL] Brooks, Alice S. Lugtenberg, Dorien Lake, Jennifer Debaix, Huguette Rudin, Christoph Knebelmann, Bertrand Tellier, Stephanie Rousset-Rouvière, Caroline Viering, Daan de Baaij, Jeroen H. F. Weber, Stefanie Palygin, Oleg Staruschenko, Alexander Kleta, Robert Houillier, Pascal Bockenhauer, Detlef Devuyst, Olivier[UCL] Vargas-Poussou, Rosa Warth, Richard Zdebik, Anselm A. Konrad, Martin (2021) Journal of the American Society of Nephrology — Vol. 32, no. 6, p. 1498-1512 (2021)
    • Journal article
    INNOVATIONS EN Néphrologie QUE RETENIR DE 2016 ?
    Demoulin, Nathalie[UCL] Anh Ho[UCL] Godefroid, Nathalie[UCL] Clerckx Caroline[UCL] Annet, Laurence[UCL] Pirson, Yves[UCL] Devuyst, Olivier[UCL] Jadoul, Michel[UCL] Aydin, Selda[UCL] Goletti Sylvie[UCL] Morelle, Johann[UCL] Goffin, Eric[UCL] Mourad, Michel[UCL] (2017) Louvain médical — Vol. 136, no.2, p. 103-109 (2017)
    • Journal article
    Monogenic Kidney Diseases in Kidney Transplantation
    Gillion, Valentine[UCL] Devresse, Arnaud[UCL] Olinger, Eric[UCL] Dahlqvist, Géraldine[UCL] Demoulin, Nathalie[UCL] Godefroid, Nathalie[UCL] Claes, Kathleen Devuyst, Olivier[UCL] Kanaan, Nada[UCL] (2023) Kidney International Reports — (2023)
    • Speech
    Syndrome de Gitelman et protéinurie glomérulaire: à propos d'une association atypique
    Demoulin, Nathalie[UCL] Cosyns, Jean-Pierre[UCL] Cornet, C. Godefroid, Nathalie[UCL] Pirson, Yves[UCL] Jadoul, Michel[UCL] Dahan, Karin[UCL] Devuyst, Olivier[UCL] (2010) 12e Réunion commune de la Société de Néphrologie (SN) et de la Société Francophone de Dialyse (SFD) — (Belgium) Brussels
    • Journal article
    Transcriptional and functional analyses of SLC12A3 mutations: new clues for the pathogenesis of Gitelman syndrome.
    Riveira-Munoz, Eva[UCL] Chang, Qing Godefroid, Nathalie[UCL] Hoenderop, Joost G. Bindels, René J Dahan, Karin[UCL] Devuyst, Olivier[UCL] (2007) Journal of the American Society of Nephrology : JASN — Vol. 18, no. 4, p. 1271-83 (2007)
    • Journal article
    Prevalence of Hypertension in Children with Early-Stage ADPKD
    Massella, Laura Mekahli, Djalila Paripović, Dušan Prikhodina, Larisa Godefroid, Nathalie[UCL] Niemirska, Anna Ağbaş, Ayşe Kalicka, Karolina Jankauskiene, Augustina Mizerska-Wasiak, Malgorzata Afonso, Alberto Caldas Salomon, Rémi Deschênes, Georges Ariceta, Gema Özçakar, Z. Birsin Teixeira, Ana Duzova, Ali Harambat, Jérôme Seeman, Tomáš Hrčková, Gabriela Lungu, Adrian Catalin Papizh, Svetlana Peco-Antic, Amira De Rechter, Stéphanie Giordano, Ugo Kirchner, Marietta Lutz, Teresa Schaefer, Franz Devuyst, Olivier[UCL] Wühl, Elke Emma, Francesco (2018) Clinical Journal of the American Society of Nephrology — Vol. 13, no. 6, p. 874-883 (2018)
    • Journal article
    Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies
    Ashton, Emma J. Legrand, Anne Benoit, Valerie Roncelin, Isabelle Venisse, Annabelle Zennaro, Maria-Christina Jeunemaitre, Xavier Iancu, Daniela van’t Hoff, William G. Walsh, Stephen B. Godefroid, Nathalie[UCL] Rotthier, Annelies Del Favero, Jurgen Devuyst, Olivier[UCL] Schaefer, Franz Jenkins, Lucy A. Kleta, Robert Dahan, Karin[UCL] Vargas-Poussou, Rosa Bockenhauer, Detlef (2018) Kidney international — Vol. 93, no. 4, p. 961-967 (2018)
    • Speech
    A new class of mutations involved in Gitelman's syndrome affects the intrinsic activity of the Na-Cl cotransporter NCCT
    Riveira-Munoz, Eva[UCL] Dahan, Karin[UCL] Godefroid, Nathalie[UCL] Devuyst, Olivier[UCL] Chang, Qing Hoenderop, Joost G. Bindels, Rene (2006) 43rd ERA-EDTA Congress — Glasgow (Scotland)
    • Journal article
    HNF1ß: A gene, several phenotypes
    Ho, Thien Anh[UCL] Godefroid, Nathalie[UCL] Devuyst, Olivier[UCL] Pirson, Yves[UCL] Demaret, Tanguy[UCL] Dahan, Karin[UCL] (2014) Louvain médical — Vol. 133, no. 4, p. 197-200 (2014)
    • Journal article
    Autosomal dominant polycystic kidney disease is associated with central and nephrogenic defects in osmoregulation.
    Ho, Thien Anh[UCL] Godefroid, Nathalie[UCL] Gruzon, Damien[UCL] Haymann, Jean-Philippe Maréchal, Céline[UCL] Wang, Xueqi Serra, Andreas Pirson, Yves[UCL] Devuyst, Olivier[UCL] (2012) Kidney International — Vol. 82, no. 10, p. 1121-1129 (2012)